A method of rapidly detecting trace materials including biohazards, toxins, radioactive materials, and narcotics in situ is disclosed. A corresponding apparatus is disclosed. A trace of the material is collected on a pad of the card component, collected by swiping the pad on suspected surface or exposure to the suspected air volume. A novel card component is disclosed that when inserted in a chemical detection unit (CDU), releases reaction chemicals from flexible walled capsules in desired sequence. The exposed pad containing trace material and chemicals are heated in the chemical detection unit to produce a spectral pattern that is analyzed by the optical electronics in the CDU and results are displayed, stored and/or transmitted over a communications network.
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1. A system of detecting unknown trace compounds, the system comprising a card component and a chemical detection unit:
wherein the card component comprises:
i. a backing plate;
ii. a pad mounted on the backing plate for acquiring a sample of unknown chemical;
iii. at least one flexible walled capsule attached to the backing plate for storage of reaction compounds,
wherein the at least one flexible walled capsule is capable of establishing fluid communication with the pad, and
wherein the at least one flexible walled capsule is adapted to yield to establish fluid communication between reaction compounds and the pad when the card component is coupled to the chemical detection unit; and
iv. a cover, covering the card component;
wherein the chemical detection unit is adapted for use in conjunction with the card component, and wherein the chemical detection unit comprises:
a housing comprising a card ingress cavity,
wherein the housing is adapted to couple with the card component through the card ingress cavity,
wherein an interior wall of the card ingress cavity comprises a raised surface adapted to couple with the card component through application of compressive force to the at least one flexible walled capsule,
wherein coupling of the card component with the card ingress cavity causes at least one wall of the at least one flexible walled capsule to yield to cause fluid flow from the at least one flexible walled capsule and thereby establish fluid communication between the pad and fluids in the at least one flexible walled capsule.
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This application is a divisional of U.S. patent application Ser. No. 12/309,704, filed on Jan. 26, 2009, which claims priority to provisional application No. 60/833,727, filed on Jul. 26, 2006, which are herein incorporated by reference in their entirety.
Not Applicable.
Not Applicable.
1. Field of the Invention
The invention described herein relates generally to a method and apparatus for the detection of chemicals and biological agents. More specifically, it relates to a handheld electronic device and a card that can be used to collect and qualify or quantify chemicals in the environment. The invention is composed of two components, an electronic device with an optical system that can read, interpret and display a range of colors developed on a pad and a card containing said pad and incorporating liquid reagent capsules that can be activated in a controlled sequence, heated, or dried, and used to generate a pattern of colors specific to a limited range of chemicals.
2. Description of the Related Art
There is a desperate need for an improved method for detecting trace levels of certain chemicals. This is best exemplified by the recent terrorist bombings that have occurred in many countries across the globe.
Thousands of soldiers and civilians have been killed and tens of thousands wounded by what are commonly known as Improvised Explosive Devices or IED's. They range from homemade explosives formed from commercially available compounds such as peroxide and acetone that were used in the second set of London bombings in 2006; to more sophisticated devices made from virtually undetectable explosives like “Semtex” and incorporating explosive formed charges.
The latter has proved to be a particularly effective killing tool in which high explosive is place below a shaped metal disk. A mobile phone or wired detonator is embedded in the explosive, which is then detonated from a remote location. The metal disk melts by the explosion and forms a liquid projectile capable of penetrating inches of steel armor plating.
Despite the impression created by various sources in public mind, there is no way to detect these explosive devices once made and hidden by the roadside. As reported by a Department of Justice Study, the variety of high explosive used by the terrorists do not produce a vapor and cannot be detected by vapor based chemical sensors sometimes referred to as “sniffers” or by canine units.
Furthermore there is no way to effectively detect or block the use of the mobile phone as an effective detonator. In addition, the “Humvees” and like vehicles used for protecting soldiers, cannot carry sufficient armor plating to prevent penetration by the explosive formed charges. In short, we have no effective weapon against these devices.
The matter is further complicated by the peroxide types of explosives where the components are found in nail polish and cleaning fluid. Though these compounds are easily detected by vapor, they are ubiquitous making vapor detection useless.
In a significant but less dramatic setting we lack effective portable devices for identifying traces of many other compounds such as narcotics and biological agents. Biological agents range from those organisms that could be used for bio-terror such as Anthrax spores, to important causes of food poisoning. Several incidents have occurred recently with the contamination of spinach and peanut butter where a hand held portable detector would have permitted more rapid identification and eradication of the source.
It is argued that X-ray screening of baggage is an effective deterrent to those who would try to bomb a plane but it is equally apparent that detonation of a high explosive anywhere in the airport terminal would cause as much death and disruption as detonating the explosive on the plane.
Recent events in Glasgow, Scotland illustrated this whereby the explosive device was in a car that drove into the airport terminal and would not have been detected by existing methods. Use of a hand held portable device would permit establishing a “presence” for security personnel outside the confines of the baggage screening areas providing an improved deterrent.
For trace chemical detection there are physical methods and chemical methods. Physical methods involve the interaction of the vaporized molecule with an electronic detector. One common method referred to as Ion Mobility Spectroscopy or IMS is as follows. A sample is collected onto a swipe pad. The pad is then placed in a powerful electric field or near a radiation source and the sample molecules are broken up into ions, which are smaller electrically charged fragments. These ions are then electrically accelerated into a tube against a flow of inert gas. The gas slows the ions down and they fall onto electronic detectors. How far they progress down the tube is determined by the ion's size and charge.
If a sample of TNT is collected, ionized and passed down the tubes, its component parts will fall onto the detectors at specific locations which are stored by the machine. If an unknown compound thought to be TNT is collected and ionized, and if the gas flow rate and electrical acceleration are not altered, then the particles should fall in the same locations in similar proportions and the machine will detect it as TNT.
These machines are extremely sensitive and powerful laboratory tools. However, they do not perform as well when used a screening tool due to fluctuations in atmospheric pressure, high concentrations of benign compounds, and the overall complexity of the device. These common variables cause the device to alarm when there is no explosive present or worse yet, miss a real explosive. In addition these devices require a gas supply, are heavy, expensive, and require up to 20 minutes of calibration and warm-up time before use.
A further physical method involves the use of a selective polymer to bind the explosive as the vapor passes across a sensor. This binding induces physicals change such as how it interacts with light or a microscopic increase in weight, which is then detected electronically. These devices have also proved ineffective in real world settings because there are millions of similar molecules in the environment. Some of these molecules are present in very high concentrations, and these “like” compounds non-specifically bind to the polymer and are detected or block the detection of the real agent.
To be effective in detecting many of the explosives, the sample must first be collected onto a swipe and then vaporized to travel across the sensor. To be at all effective, the binding chemicals must be able to bind only a very limited subset of molecules in a narrow range of concentration. A large sample of real compound will overwhelm the detector and require the device to be taken out of service and cleaned before continued use.
All of the physical methods require large, less portable machines, frequent calibration, extensive training and are generally expensive; costing more than $US30,000 per unit. Though the actual analysis may take only seconds, the warm up time and calibration and repeat calibration commonly require 30 minutes to run 10 samples.
At times, for effective detection in existing methods, samples must be diluted to the effective detection range of the device, requiring preceding knowledge of the sample or repeated testing, as well as advanced expertise in this procedure.
These devices are very prone to error if moved or exposed to varying temperatures. Most systems have electrical requirements of 120 VAC and have significant consumables such as gas canisters and replacement sensors.
Chemical methods are less varied. Essentially, for the detection of explosive compounds, these methods all use a similar group of chemicals that have been published in chemistry texts for decades. These chemicals react in a liquid medium with certain functional groups on the explosives and produce an observable color change.
Similar color chemistry methods exist for narcotics and many biological molecules. In addition, specific antibodies can be labeled with a color tag and bound to the target molecules in a liquid medium. The most common example of which is the ubiquitous urine pregnancy test.
Until the present invention, chemical methods were both hazardous to perform and technically difficult to execute. They required the application of caustic and acidic compounds and heat to the test pad to produce subtle color changes that were difficult to interpret correctly by eye. Existing embodiments of the method involve the spraying on of reagents, dropping of reagents from a dropper bottle or the crushing a glass ampoule.
In some versions, the operator must adjust the procedure based on initial results. In other embodiments, operators must time the procedure carefully and ignore specific colors even if they are the correct color but develop at the wrong time. All the existing embodiments are read by human eye and are subject to error from individual color perception, ambient lighting and temperature conditions.
By way of example, one such existing color chemistry method involves the spraying of the first reagent onto a paper swipe. If no color develops or if the color is not from a selected limited grouping, then a second reagent is sprayed. Depending on the timing and color that then may be produced, a third reagent may be added. If left, the paper swipe will develop a color change itself, which must be ignored. All these changes are dramatically affected by the accuracy of spraying and the ambient temperature.
In another embodiment, the user must add drops of solution from a bottle. A timer controls the heat reaction and a pink or orange coloration indicates a positive result for some explosives, however, gray and purple colors do not. Unfortunately these colors may be produced in the presence of common compounds such as red wine or ink, and incorrectly interpreted as a positive result. If no pink or orange color develops, the second reagent is added and the heat reapplied. Again, if particular colors develop it is a positive detection, but the presence of other colors are not. The interpretation of these colors, particularly in strong or weak lighting conditions, can completely obfuscate a positive result. Additionally, the reagents deteriorate in the bottles with exposure to air, and are extremely astringent, requiring the operator to wear personal protective equipment at all times, such as safety goggles and gloves.
A better understanding of the present invention can be obtained when the following detailed description of some embodiments is considered in conjunction with the drawings of the above noted application and the following drawings in which:
The present invention alleviates the above noted problems by providing a simple, hand held, battery powered, sensitive and specific unit requiring no external calibration, ability to work in a wide range of environments, with a broad dynamic range and “plug-and-play” type operation. The flexible capsules contained in the card safely enclose and protect the reagents. Once swiped on a surface and placed in the machine, the device controls the sequence of fluid addition and heating. The optical assembly provides controlled illumination at specific wavelengths, any of which can be turned on separately by the controlling software.
The detector incorporates software configurable color filters and detects specific wavelengths in and beyond the human-visible spectrum, permitting an objective and sensitive measurement of color. If desired, the device can work fluoroscopically using different illuminating and detecting wavelengths.
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If download option for downloading data from the CDU to a computer or other device is selected, a download target menu 60 is presented to the user. The download target may be a computer or an SD card or any other suitable device. A transmit data is requested 62 and after the transmission is successfully completed the user is directed to the main menu.
If the review of test result data is desired a prompt to scan or review results 16 is presented. If scan option is selected, trigger barcode reading prompt 15 is issued. The corresponding data for the barcode ID is searched 18 and card results 50 are displayed and the user is taken back to the main menu. If review option is selected, the results for each bar coded card 50 are presented upon request. After completing the review the user is taken back to the main menu.
The use of liquid chemistry in this way greatly improves the specificity of the device as the selected chemicals will only produce a pattern of certain colors with a limited set of molecules. Therefore all other molecules, even in large concentration, will not produce the same color pattern over the cycle. For some compounds such as biological agents, only a single reagent may be needed to produce a color. In many cases the fluid acts as a carrier and medium in which an antigen-antibody binding event takes place. In a further embodiment the reaction pad can be divided into three separate fluid channels each in proximity to a specific capsule. In this way three separate color reactions can be produced spatially in a side-by-side configuration rather than in timed sequence. The physical pattern of colors rather than the timed sequence of color development is equally specific for the chemicals of interest.
By way of example for the screening for trace explosives in its simplest embodiment, the user simply swipes the card on the surface to under test, places it into the chemical reader, and the liquid chemistry and colorimetric analysis are all performed and the result displayed within a short time.
Once the sample is collected and the bar code interpreted, the card is inserted into the device. In one preferred embodiment the card contains two embedded capsules that contain relevant chemicals. The color of the pad is recorded by the device as background and for later analysis. The first capsule is activated and any sequence of color changes is recorded. For macroscopic samples a color may develop for certain explosives immediately. For example, the explosive TNB (tri nitro benzene) will produce an orange coloration. One of the advantages of the method is that it can operate with samples ranging from the macroscopic (milligram) level to the trace (nanogram) level. For a trace sample no color will develop initially, but will appear when heat is applied to the reaction pad. For TNB an orange tinge will develop, but for the explosive HMX no color will appear. The second capsule is then activated and the color recorded. For TNB the color will transition from orange to clear. For macroscopic samples of HMX a pink color will appear, however for trace levels there may be no color change. Heat is then added to the reaction pad and as an example, a pink color would develop for trace amounts of HMX.
The color, sequence, and rate of change of development of the colors is specific for each analyte or related group.
Pigments and dirt may easily be collected from a surface and are easily ignored as they do not produce a color change through the cycle. Substances that do change color will do so in a different manner than targeted substances, as they do not belong to the same chemical groups (families) as the explosive.
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The barcode reader could also be used to collect information from specific sites or objects separately labeled. By way of example a barcode could be placed in a specific location such that when the Chemical Detector Unit is placed in front of it to read the code, it provides location and orientation information. Subsequently, other barcodes could be placed in strategic locations to provide further information.
By way of example, a “first responder” could enter a building whereby scanning of a specifically located barcode provides the starting point for tracking position. Upon entering another floor additional barcodes attached at specific locations could provide information regarding that location within a building.
In a further embodiment of the device the Chemical Detection Unit includes a “radio frequency identification”, or RFID, reader. RFID tags attached at specific locations could be read as the device approached, providing location information. Another example would be to replace the barcode scanner and associated procedures and utilize RFID tags implanted into the card component for card identification.
In further embodiments of the device the card can be placed into a separate apparatus to enhance sample collection. Examples include a wand, permitting the card to be swiped behind a cupboard or hard to reach location, an air concentrator device which could collect particles in the air and propel them onto the swipe area, or the card itself could be incorporated into the body of a box cutter type blade and slid into cardboard boxes, SHEETROCK walls (i.e., drywalls), or other penetrable surfaces.
In further embodiments of the device the Chemical Detection Unit could incorporate a radiation detection sensor or toxic vapor detection sensor of which there are many variations. The detailed invention is the subject of a separate application. By way of example this device could continuously monitor for other toxic and radiation hazards while simultaneously being used to detect trace chemicals.
In a further embodiment of the device, the wireless Bluetooth feature could be paired with a common headset typically used for cellular telephone applications. This headset would provide audible resources to the user, and also allow the user to record audio for storage on the device. An example would be to play back to the user a stored audio recording of a chemical description associated with a test result. Another example would be to permit the operator to record vocal notes to be stored along with the test results in the device. Further examples would be for use with the help system for audio instructions, or for step-by-step feedback from the device to the operator during use.
In a further embodiment of the device, electronic capabilities will be included to communicate over various wireless communication networks. These networks would include, but are not limited to, digital cellular phone networks (EDGE, CDMA, etc.), IEEE 802.11x (Wi-Fi) networks, Zigbee, and SMS text networks. An example would be to send an SMS text to a central reporting location after each positive detection of an explosive. Another example would be to send result and GPS location data over the Internet to a data center which could map positive results from clusters of devices to geo-locate ‘hot spot’ regions to better focus military resources into a given geographical area.
In further embodiments of the device, the Bluetooth wireless networking feature could be used to form a personal area network (PAN) to communicate location and result data among multiple devices or to a central base station. This base station could be fitted with a printer and other peripherals, which would allow for group use of multiple devices in facilities with pre-existing security procedures to allow for replacement of existing trace detection systems. Another example would be for multiple devices to function in a ‘team’ mode for transmitting messages, test results, audio communication and geo-location among preset groups of devices.
In further embodiments of the device, peripheral devices will be connected wirelessly via Bluetooth. An example of this would be a portable radiation detector, which would integrate into the user interface of the device to expand the detection capabilities of the device. As an additional example, the radiation detection and GPS positioning would allow for directional determination of radiation sources. By measuring the radiation strength at multiple locations, one could direct the user towards the radioactive source. When using the ‘team’ pairing mode of multiple CDU devices, additional source, direction and magnitude measurements would be compiled to increase the accuracy of the radiation source location.
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The foregoing disclosure and description of the preferred embodiments are illustrative and explanatory thereof, and various changes in the components, elements, configurations, and signal connections, as well as in the details of the illustrated apparatus and construction and method of operation may be made without departing from the spirit and scope of the invention and within the scope of the claims.
Clift, Vaughan L., Harriman, Kristin L., Pettys, Richard L., Headley, David M., Conerly, Tiffany M.
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Sep 23 2010 | CLIFT, VAUGHAN L | DETECTACHEM | ASSIGNMENT OF ASSIGNORS INTEREST SEE DOCUMENT FOR DETAILS | 034798 | /0967 | |
Sep 23 2010 | HARRIMAN, KRISTIN L | DETECTACHEM | ASSIGNMENT OF ASSIGNORS INTEREST SEE DOCUMENT FOR DETAILS | 034798 | /0967 | |
Jan 20 2011 | CONERLY, TIFFANY M | DETECTACHEM | ASSIGNMENT OF ASSIGNORS INTEREST SEE DOCUMENT FOR DETAILS | 034798 | /0967 | |
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Mar 18 2015 | PETTYS, RICHARD L | DETECTACHEM | ASSIGNMENT OF ASSIGNORS INTEREST SEE DOCUMENT FOR DETAILS | 035224 | /0259 | |
Mar 18 2015 | HEADLEY, DAVID M | DETECTACHEM | ASSIGNMENT OF ASSIGNORS INTEREST SEE DOCUMENT FOR DETAILS | 035224 | /0259 | |
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